FDA UDI Not in Commercial Distribution 🇺🇸 United States

KALIX II

DI: 10381780048152 · Model: 141009ND · NEWDEAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
KALIX II
Primary DI
10381780048152
Version / Model
141009ND
Catalog Number
141009ND
Company Name
NEWDEAL
Labeler DUNS
536935331
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
3af475c3-c6a7-4b7b-8193-49cf18df7294
Distribution End Date
2016-02-11

Device Description

The KALIX II Flat Foot implant is a combination of three sterile components. Two of them are made from Titanium alloy, and the outer sleeve is made from Ultra High Molecular Weight Polyethylene. The implant is indicated for use in the treatment of the hyperpronated foot and stabilization of the subtalar joint. It is designed to block forward, downward and medial displacement of the talus, thus allowing normal subtalar joint motion but blocking excessive pronation and the resulting sequela. Available in different sizes.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWC Screw, fixation, bone

GMDN Terms

Code Name
40352 Subtalar implant, non-bioabsorbable

Identifiers

Type ID
Primary 10381780048152
Secondary M248141009ND1

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 9mm diameter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in dry place.